THE BODYGUARDS ULTRA POW-FREE HYPO LATEX EXAM GLOV
K-Number: K924909 · 1993-05-17
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Device Summary
Frequently Asked Questions
What is the THE BODYGUARDS ULTRA POW-FREE HYPO LATEX EXAM GLOV?
THE BODYGUARDS ULTRA POW-FREE HYPO LATEX EXAM GLOV is a medical device that received FDA 510(k) clearance on 1993-05-17. The listed applicant is T.K. Glove Products Co., Ltd.. The 510(k) number is K924909.
When did THE BODYGUARDS ULTRA POW-FREE HYPO LATEX EXAM GLOV receive FDA 510(k) clearance?
THE BODYGUARDS ULTRA POW-FREE HYPO LATEX EXAM GLOV received FDA 510(k) clearance on 1993-05-17, under 510(k) number K924909.
Who is the listed applicant for THE BODYGUARDS ULTRA POW-FREE HYPO LATEX EXAM GLOV?
The FDA 510(k) record lists T.K. Glove Products Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for THE BODYGUARDS ULTRA POW-FREE HYPO LATEX EXAM GLOV?
The FDA product code for THE BODYGUARDS ULTRA POW-FREE HYPO LATEX EXAM GLOV is LYY.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing T.K. Glove Products Co., Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: LYY)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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